AU722731B2 - Heteroatom substituted metallocene compounds for olefin polymerization catalyst systems and methods for preparing them - Google Patents

Heteroatom substituted metallocene compounds for olefin polymerization catalyst systems and methods for preparing them Download PDF

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Publication number: AU722731B2
Authority: AU; Australia
Prior art keywords: group; indene; polymerization; tri; tert
Prior art date: 1996-01-30
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Ceased

Application number

AU15485/97A

Other languages

English (en)

Other versions

AU1548597A (en

Inventor

Reko Leino

Hendrik Luttikhedde

Jan Nasman

Carl-Erik Wilen

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Borealis AS

Original Assignee

Borealis AS

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1996-01-30

Filing date

1997-01-30

Publication date

2000-08-10

1997-01-30 Application filed by Borealis AS filed Critical Borealis AS

1997-08-22 Publication of AU1548597A publication Critical patent/AU1548597A/en

2000-08-10 Application granted granted Critical

2000-08-10 Publication of AU722731B2 publication Critical patent/AU722731B2/en

2017-01-30 Anticipated expiration legal-status Critical

Status Ceased legal-status Critical Current

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238000000034 method Methods 0.000 title claims description 10
150000001336 alkenes Chemical class 0.000 title claims description 8
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 title claims description 3
239000002685 polymerization catalyst Substances 0.000 title claims description 3
150000001875 compounds Chemical class 0.000 title description 44
125000005842 heteroatom Chemical group 0.000 title description 3
238000006116 polymerization reaction Methods 0.000 claims description 76
YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Natural products C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 claims description 44
239000003054 catalyst Substances 0.000 claims description 43
238000006243 chemical reaction Methods 0.000 claims description 43
-1 tetrahydroindenyl Chemical group 0.000 claims description 41
MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 claims description 31
239000002904 solvent Substances 0.000 claims description 26
239000003446 ligand Substances 0.000 claims description 23
125000003454 indenyl group Chemical group C1(C=CC2=CC=CC=C12)* 0.000 claims description 19
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 12
125000003118 aryl group Chemical group 0.000 claims description 11
125000005843 halogen group Chemical group 0.000 claims description 11
229910052710 silicon Inorganic materials 0.000 claims description 10
125000000217 alkyl group Chemical group 0.000 claims description 9
125000004429 atom Chemical group 0.000 claims description 9
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 8
239000012018 catalyst precursor Substances 0.000 claims description 8
239000010703 silicon Substances 0.000 claims description 8
QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 7
229910052726 zirconium Inorganic materials 0.000 claims description 7
125000003710 aryl alkyl group Chemical group 0.000 claims description 6
125000001183 hydrocarbyl group Chemical group 0.000 claims description 6
239000001257 hydrogen Substances 0.000 claims description 6
229910052739 hydrogen Inorganic materials 0.000 claims description 6
UMJJFEIKYGFCAT-UHFFFAOYSA-N indan-2-one Chemical compound C1=CC=C2CC(=O)CC2=C1 UMJJFEIKYGFCAT-UHFFFAOYSA-N 0.000 claims description 6
229910052723 transition metal Inorganic materials 0.000 claims description 6
150000003624 transition metals Chemical class 0.000 claims description 6
RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 5
125000003545 alkoxy group Chemical group 0.000 claims description 5
238000007334 copolymerization reaction Methods 0.000 claims description 5
229910052732 germanium Inorganic materials 0.000 claims description 5
GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 claims description 5
229910052751 metal Inorganic materials 0.000 claims description 5
239000002184 metal Substances 0.000 claims description 5
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
229910052719 titanium Inorganic materials 0.000 claims description 5
239000010936 titanium Substances 0.000 claims description 5
AQZWEFBJYQSQEH-UHFFFAOYSA-N 2-methyloxaluminane Chemical compound C[Al]1CCCCO1 AQZWEFBJYQSQEH-UHFFFAOYSA-N 0.000 claims description 4
125000003342 alkenyl group Chemical group 0.000 claims description 4
239000000460 chlorine Substances 0.000 claims description 4
125000001309 chloro group Chemical group Cl* 0.000 claims description 4
229910052735 hafnium Inorganic materials 0.000 claims description 4
VBJZVLUMGGDVMO-UHFFFAOYSA-N hafnium atom Chemical compound [Hf] VBJZVLUMGGDVMO-UHFFFAOYSA-N 0.000 claims description 4
125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 claims description 4
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
125000002877 alkyl aryl group Chemical group 0.000 claims description 3
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 3
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
229910052801 chlorine Inorganic materials 0.000 claims description 2
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 2
125000004639 dihydroindenyl group Chemical group C1(CCC2=CC=CC=C12)* 0.000 claims description 2
230000000737 periodic effect Effects 0.000 claims description 2
239000002243 precursor Substances 0.000 claims description 2
125000006657 (C1-C10) hydrocarbyl group Chemical group 0.000 claims 1
CCPHAMSKHBDMDS-UHFFFAOYSA-N Chetoseminudin B Natural products C=1NC2=CC=CC=C2C=1CC1(SC)NC(=O)C(CO)(SC)N(C)C1=O CCPHAMSKHBDMDS-UHFFFAOYSA-N 0.000 claims 1
241000208152 Geranium Species 0.000 claims 1
HCFQDMDVMBTQOR-UHFFFAOYSA-N [SiH3]OC1=Cc2ccccc2C1 Chemical compound [SiH3]OC1=Cc2ccccc2C1 HCFQDMDVMBTQOR-UHFFFAOYSA-N 0.000 claims 1
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 54
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical class CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 36
CPOFMOWDMVWCLF-UHFFFAOYSA-N methyl(oxo)alumane Chemical compound C[Al]=O CPOFMOWDMVWCLF-UHFFFAOYSA-N 0.000 description 29
239000011541 reaction mixture Substances 0.000 description 29
238000005481 NMR spectroscopy Methods 0.000 description 28
OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 28
230000000694 effects Effects 0.000 description 25
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 24
239000005977 Ethylene Substances 0.000 description 24
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 24
229920000642 polymer Polymers 0.000 description 22
VPGLGRNSAYHXPY-UHFFFAOYSA-L zirconium(2+);dichloride Chemical compound Cl[Zr]Cl VPGLGRNSAYHXPY-UHFFFAOYSA-L 0.000 description 22
239000000203 mixture Substances 0.000 description 18
101150041968 CDC13 gene Proteins 0.000 description 16
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 16
HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 16
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
DLEDOFVPSDKWEF-UHFFFAOYSA-N lithium butane Chemical compound [Li+].CCC[CH2-] DLEDOFVPSDKWEF-UHFFFAOYSA-N 0.000 description 13
239000003921 oil Substances 0.000 description 13
235000019198 oils Nutrition 0.000 description 13
229910052938 sodium sulfate Inorganic materials 0.000 description 13
235000011152 sodium sulphate Nutrition 0.000 description 13
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 12
KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 12
239000004698 Polyethylene Substances 0.000 description 11
238000001704 evaporation Methods 0.000 description 11
230000008020 evaporation Effects 0.000 description 11
239000007787 solid Substances 0.000 description 11
238000001816 cooling Methods 0.000 description 10
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 9
229910007926 ZrCl Inorganic materials 0.000 description 9
RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 9
239000012074 organic phase Substances 0.000 description 9
238000005160 1H NMR spectroscopy Methods 0.000 description 8
239000000843 powder Substances 0.000 description 8
239000000725 suspension Substances 0.000 description 8
APQIUTYORBAGEZ-UHFFFAOYSA-N 1,1-dibromoethane Chemical compound CC(Br)Br APQIUTYORBAGEZ-UHFFFAOYSA-N 0.000 description 7
238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 7
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical class [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 7
238000001819 mass spectrum Methods 0.000 description 7
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 7
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 7
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
239000012190 activator Substances 0.000 description 6
150000002500 ions Chemical class 0.000 description 6
DUNKXUFBGCUVQW-UHFFFAOYSA-J zirconium tetrachloride Chemical compound Cl[Zr](Cl)(Cl)Cl DUNKXUFBGCUVQW-UHFFFAOYSA-J 0.000 description 6
PEJJRWHRMLPGDG-UHFFFAOYSA-N 1h-inden-2-yloxy-dimethyl-(2-methylpentan-2-yl)silane Chemical compound C1=CC=C2CC(O[Si](C)(C)C(C)(C)CCC)=CC2=C1 PEJJRWHRMLPGDG-UHFFFAOYSA-N 0.000 description 5
OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 5
230000000052 comparative effect Effects 0.000 description 5
239000013078 crystal Substances 0.000 description 5
125000002524 organometallic group Chemical group 0.000 description 5
VVAXKNLRUHHJCZ-UHFFFAOYSA-N tert-butyl-(1h-inden-2-yloxy)-dimethylsilane Chemical compound C1=CC=C2CC(O[Si](C)(C)C(C)(C)C)=CC2=C1 VVAXKNLRUHHJCZ-UHFFFAOYSA-N 0.000 description 5
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
238000002425 crystallisation Methods 0.000 description 4
230000008025 crystallization Effects 0.000 description 4
238000004821 distillation Methods 0.000 description 4
239000000047 product Substances 0.000 description 4
QMYBXECXCNZHMM-UHFFFAOYSA-N tert-butyl-(1h-inden-2-yloxy)-diphenylsilane Chemical compound C=1C2=CC=CC=C2CC=1O[Si](C(C)(C)C)(C=1C=CC=CC=1)C1=CC=CC=C1 QMYBXECXCNZHMM-UHFFFAOYSA-N 0.000 description 4
XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 3
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
235000019502 Orange oil Nutrition 0.000 description 3
239000004743 Polypropylene Substances 0.000 description 3
FSLSKEFNMQRNRQ-UHFFFAOYSA-N [1-[1-[2-[dimethyl(2-methylpentan-2-yl)silyl]oxy-1h-inden-1-yl]ethyl]-1h-inden-2-yl]oxy-dimethyl-(2-methylpentan-2-yl)silane Chemical compound CCCC(C)(C)[Si](C)(C)OC1=CC2=CC=CC=C2C1C(C)C1C2=CC=CC=C2C=C1O[Si](C)(C)C(C)(C)CCC FSLSKEFNMQRNRQ-UHFFFAOYSA-N 0.000 description 3
MIVGNBLEYFDVMG-UHFFFAOYSA-N cyclohexyl-(1h-inden-2-yloxy)-dimethylsilane Chemical compound C=1C2=CC=CC=C2CC=1O[Si](C)(C)C1CCCCC1 MIVGNBLEYFDVMG-UHFFFAOYSA-N 0.000 description 3
LIKFHECYJZWXFJ-UHFFFAOYSA-N dimethyldichlorosilane Chemical compound C[Si](C)(Cl)Cl LIKFHECYJZWXFJ-UHFFFAOYSA-N 0.000 description 3
150000002362 hafnium Chemical class 0.000 description 3
125000000623 heterocyclic group Chemical group 0.000 description 3
239000000178 monomer Substances 0.000 description 3
239000010502 orange oil Substances 0.000 description 3
150000003839 salts Chemical class 0.000 description 3
125000001424 substituent group Chemical group 0.000 description 3
ODKBFKLBYDZPQS-UHFFFAOYSA-N tert-butyl-[[1-[1-[2-[tert-butyl(dimethyl)silyl]oxy-1h-inden-1-yl]ethyl]-1h-inden-2-yl]oxy]-dimethylsilane Chemical compound CC(C)(C)[Si](C)(C)OC1=CC2=CC=CC=C2C1C(C)C1C2=CC=CC=C2C=C1O[Si](C)(C)C(C)(C)C ODKBFKLBYDZPQS-UHFFFAOYSA-N 0.000 description 3
BCNZYOJHNLTNEZ-UHFFFAOYSA-N tert-butyldimethylsilyl chloride Chemical compound CC(C)(C)[Si](C)(C)Cl BCNZYOJHNLTNEZ-UHFFFAOYSA-N 0.000 description 3
KPZGRMZPZLOPBS-UHFFFAOYSA-N 1,3-dichloro-2,2-bis(chloromethyl)propane Chemical compound ClCC(CCl)(CCl)CCl KPZGRMZPZLOPBS-UHFFFAOYSA-N 0.000 description 2
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 2
125000005234 alkyl aluminium group Chemical group 0.000 description 2
229910052786 argon Inorganic materials 0.000 description 2
SZLCRBUXZGPBQK-UHFFFAOYSA-N bis[2-[tert-butyl(dimethyl)silyl]oxy-1h-inden-1-yl]-dimethylsilane Chemical compound CC(C)(C)[Si](C)(C)OC1=CC2=CC=CC=C2C1[Si](C)(C)C1C2=CC=CC=C2C=C1O[Si](C)(C)C(C)(C)C SZLCRBUXZGPBQK-UHFFFAOYSA-N 0.000 description 2
238000009835 boiling Methods 0.000 description 2
238000012512 characterization method Methods 0.000 description 2
IJOOHPMOJXWVHK-UHFFFAOYSA-N chlorotrimethylsilane Chemical compound C[Si](C)(C)Cl IJOOHPMOJXWVHK-UHFFFAOYSA-N 0.000 description 2
238000001640 fractional crystallisation Methods 0.000 description 2
239000007789 gas Substances 0.000 description 2
PDPJQWYGJJBYLF-UHFFFAOYSA-J hafnium tetrachloride Chemical group Cl[Hf](Cl)(Cl)Cl PDPJQWYGJJBYLF-UHFFFAOYSA-J 0.000 description 2
239000012535 impurity Substances 0.000 description 2
239000000463 material Substances 0.000 description 2
ZGEGCLOFRBLKSE-UHFFFAOYSA-N methylene hexane Natural products CCCCCC=C ZGEGCLOFRBLKSE-UHFFFAOYSA-N 0.000 description 2
125000004430 oxygen atom Chemical group O* 0.000 description 2
229920001155 polypropylene Polymers 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
229910000077 silane Inorganic materials 0.000 description 2
UOULCEYHQNCFFH-UHFFFAOYSA-M sodium;hydroxymethanesulfonate Chemical compound [Na+].OCS([O-])(=O)=O UOULCEYHQNCFFH-UHFFFAOYSA-M 0.000 description 2
230000003595 spectral effect Effects 0.000 description 2
238000006467 substitution reaction Methods 0.000 description 2
WCGLAMWRVNHSCL-UHFFFAOYSA-N tert-butyl-[[1-[1-[2-[tert-butyl(diphenyl)silyl]oxy-1h-inden-1-yl]ethyl]-1h-inden-2-yl]oxy]-diphenylsilane Chemical compound C=1C=CC=CC=1[Si](C(C)(C)C)(C=1C=CC=CC=1)OC1=CC2=CC=CC=C2C1C(C)C(C1=CC=CC=C1C=1)C=1O[Si](C(C)(C)C)(C=1C=CC=CC=1)C1=CC=CC=C1 WCGLAMWRVNHSCL-UHFFFAOYSA-N 0.000 description 2
XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical group Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 2
LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 1
KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 1
YDYCXZYKRJIHTA-UHFFFAOYSA-N 1h-inden-1-yloxygermane Chemical class C1=CC=C2C(O[GeH3])C=CC2=C1 YDYCXZYKRJIHTA-UHFFFAOYSA-N 0.000 description 1
GQNMPCODMYSQLA-UHFFFAOYSA-N 2,3-dimethylbutan-2-yl-(1h-inden-2-yloxy)-dimethylsilane Chemical compound C1=CC=C2CC(O[Si](C)(C)C(C)(C)C(C)C)=CC2=C1 GQNMPCODMYSQLA-UHFFFAOYSA-N 0.000 description 1
LSBZSFLPOXMLLB-UHFFFAOYSA-N 2,3-dimethylbutan-2-yl-[[1-[1-[2-[2,3-dimethylbutan-2-yl(dimethyl)silyl]oxy-1h-inden-1-yl]ethyl]-1h-inden-2-yl]oxy]-dimethylsilane Chemical compound CC(C)C(C)(C)[Si](C)(C)OC1=CC2=CC=CC=C2C1C(C)C1C2=CC=CC=C2C=C1O[Si](C)(C)C(C)(C)C(C)C LSBZSFLPOXMLLB-UHFFFAOYSA-N 0.000 description 1
GOJUJUVQIVIZAV-UHFFFAOYSA-N 2-amino-4,6-dichloropyrimidine-5-carbaldehyde Chemical group NC1=NC(Cl)=C(C=O)C(Cl)=N1 GOJUJUVQIVIZAV-UHFFFAOYSA-N 0.000 description 1
PUHHRKAPYINUGH-UHFFFAOYSA-N 4,7-dimethyl-1,3-dihydroinden-2-one Chemical compound CC1=CC=C(C)C2=C1CC(=O)C2 PUHHRKAPYINUGH-UHFFFAOYSA-N 0.000 description 1
DKLQZDIAQKGVTA-UHFFFAOYSA-N 4,7-dimethyl-1h-indene Chemical compound CC1=CC=C(C)C2=C1CC=C2 DKLQZDIAQKGVTA-UHFFFAOYSA-N 0.000 description 1
125000006374 C2-C10 alkenyl group Chemical group 0.000 description 1
PWAKRZXJFZFLBA-UHFFFAOYSA-N C[SiH](C)[SiH](C1C(O[Si](C)(C)C(C)(C)C)=Cc2ccccc12)C1C(O[Si](C)(C)C(C)(C)C)=Cc2ccccc12 Chemical compound C[SiH](C)[SiH](C1C(O[Si](C)(C)C(C)(C)C)=Cc2ccccc12)C1C(O[Si](C)(C)C(C)(C)C)=Cc2ccccc12 PWAKRZXJFZFLBA-UHFFFAOYSA-N 0.000 description 1
239000005046 Chlorosilane Substances 0.000 description 1
101100198507 Schizosaccharomyces pombe (strain 972 / ATCC 24843) rng2 gene Proteins 0.000 description 1
KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical group [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
238000002441 X-ray diffraction Methods 0.000 description 1
229910007928 ZrCl2 Inorganic materials 0.000 description 1
JQHPURQXTURPDS-UHFFFAOYSA-L [Cl-].[Cl-].C[Si](C)=[Zr++]([C@H]1C=CC2=C1CCCC2)[C@@H]1C=CC2=C1CCCC2 Chemical compound [Cl-].[Cl-].C[Si](C)=[Zr++]([C@H]1C=CC2=C1CCCC2)[C@@H]1C=CC2=C1CCCC2 JQHPURQXTURPDS-UHFFFAOYSA-L 0.000 description 1
239000002253 acid Substances 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
150000001450 anions Chemical class 0.000 description 1
239000012300 argon atmosphere Substances 0.000 description 1
125000005018 aryl alkenyl group Chemical group 0.000 description 1
125000004104 aryloxy group Chemical group 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
230000003197 catalytic effect Effects 0.000 description 1
238000009903 catalytic hydrogenation reaction Methods 0.000 description 1
125000002091 cationic group Chemical group 0.000 description 1
150000001768 cations Chemical class 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
KIGALSBMRYYLFJ-UHFFFAOYSA-N chloro-(2,3-dimethylbutan-2-yl)-dimethylsilane Chemical compound CC(C)C(C)(C)[Si](C)(C)Cl KIGALSBMRYYLFJ-UHFFFAOYSA-N 0.000 description 1
MEUXNEGJODESOX-UHFFFAOYSA-N chloro-cyclohexyl-dimethylsilane Chemical compound C[Si](C)(Cl)C1CCCCC1 MEUXNEGJODESOX-UHFFFAOYSA-N 0.000 description 1
KOPOQZFJUQMUML-UHFFFAOYSA-N chlorosilane Chemical class Cl[SiH3] KOPOQZFJUQMUML-UHFFFAOYSA-N 0.000 description 1
239000013065 commercial product Substances 0.000 description 1
230000009918 complex formation Effects 0.000 description 1
IDASTKMEQGPVRR-UHFFFAOYSA-N cyclopenta-1,3-diene;zirconium(2+) Chemical class [Zr+2].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 IDASTKMEQGPVRR-UHFFFAOYSA-N 0.000 description 1
125000000058 cyclopentadienyl group Chemical group C1(=CC=CC1)* 0.000 description 1
230000003247 decreasing effect Effects 0.000 description 1
YMWUJEATGCHHMB-DICFDUPASA-N dichloromethane-d2 Chemical compound [2H]C([2H])(Cl)Cl YMWUJEATGCHHMB-DICFDUPASA-N 0.000 description 1
MROCJMGDEKINLD-UHFFFAOYSA-N dichlorosilane Chemical compound Cl[SiH2]Cl MROCJMGDEKINLD-UHFFFAOYSA-N 0.000 description 1
JZZIHCLFHIXETF-UHFFFAOYSA-N dimethylsilicon Chemical group C[Si]C JZZIHCLFHIXETF-UHFFFAOYSA-N 0.000 description 1
ZSWFCLXCOIISFI-UHFFFAOYSA-N endo-cyclopentadiene Natural products C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 1
QDPBFBHDJSUOJG-UHFFFAOYSA-N ethene pentane Chemical group C=C.CCCCC QDPBFBHDJSUOJG-UHFFFAOYSA-N 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
238000001914 filtration Methods 0.000 description 1
125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 description 1
239000011521 glass Substances 0.000 description 1
238000004636 glovebox technique Methods 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
150000002367 halogens Chemical group 0.000 description 1
238000005984 hydrogenation reaction Methods 0.000 description 1
150000002469 indenes Chemical class 0.000 description 1
239000012968 metallocene catalyst Substances 0.000 description 1
DVSDBMFJEQPWNO-UHFFFAOYSA-N methyllithium Chemical group C[Li] DVSDBMFJEQPWNO-UHFFFAOYSA-N 0.000 description 1
239000012452 mother liquor Substances 0.000 description 1
YCWSUKQGVSGXJO-NTUHNPAUSA-N nifuroxazide Chemical group C1=CC(O)=CC=C1C(=O)N\N=C\C1=CC=C([N+]([O-])=O)O1 YCWSUKQGVSGXJO-NTUHNPAUSA-N 0.000 description 1
239000012299 nitrogen atmosphere Substances 0.000 description 1
238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
230000003647 oxidation Effects 0.000 description 1
238000007254 oxidation reaction Methods 0.000 description 1
YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 1
239000012071 phase Substances 0.000 description 1
NTTOTNSKUYCDAV-UHFFFAOYSA-N potassium hydride Chemical group [KH] NTTOTNSKUYCDAV-UHFFFAOYSA-N 0.000 description 1
229910000105 potassium hydride Chemical group 0.000 description 1
239000002516 radical scavenger Substances 0.000 description 1
125000006413 ring segment Chemical group 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
125000004469 siloxy group Chemical group [SiH3]O* 0.000 description 1
239000002002 slurry Substances 0.000 description 1
239000012312 sodium hydride Chemical group 0.000 description 1
229910000104 sodium hydride Inorganic materials 0.000 description 1
239000007858 starting material Substances 0.000 description 1
230000000707 stereoselective effect Effects 0.000 description 1
238000003756 stirring Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
BLTUJPISBOAJCN-UHFFFAOYSA-N tert-butyl-(1h-cyclopenta[l]phenanthren-2-yloxy)-dimethylsilane Chemical compound C12=CC=CC=C2C2=CC=CC=C2C2=C1CC(O[Si](C)(C)C(C)(C)C)=C2 BLTUJPISBOAJCN-UHFFFAOYSA-N 0.000 description 1
XBAPTBZSXHMGFX-UHFFFAOYSA-N tert-butyl-[[3-[1-[2-[tert-butyl(dimethyl)silyl]oxy-3-trimethylsilyl-3h-inden-1-yl]ethyl]-1-trimethylsilyl-1h-inden-2-yl]oxy]-dimethylsilane Chemical compound C1=CC=C2C(C(C=3C4=CC=CC=C4C(C=3O[Si](C)(C)C(C)(C)C)[Si](C)(C)C)C)=C(O[Si](C)(C)C(C)(C)C)C([Si](C)(C)C)C2=C1 XBAPTBZSXHMGFX-UHFFFAOYSA-N 0.000 description 1
MHYGQXWCZAYSLJ-UHFFFAOYSA-N tert-butyl-chloro-diphenylsilane Chemical compound C=1C=CC=CC=1[Si](Cl)(C(C)(C)C)C1=CC=CC=C1 MHYGQXWCZAYSLJ-UHFFFAOYSA-N 0.000 description 1
CZDYPVPMEAXLPK-UHFFFAOYSA-N tetramethylsilane Chemical compound C[Si](C)(C)C CZDYPVPMEAXLPK-UHFFFAOYSA-N 0.000 description 1
150000003613 toluenes Chemical class 0.000 description 1
239000004711 α-olefin Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F17/00—Metallocenes
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F110/00—Homopolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F110/02—Ethene
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F110/00—Homopolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F110/04—Monomers containing three or four carbon atoms
- C08F110/06—Propene
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F4/00—Polymerisation catalysts
- C08F4/42—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors
- C08F4/44—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides
- C08F4/60—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
- C08F4/62—Refractory metals or compounds thereof
- C08F4/64—Titanium, zirconium, hafnium or compounds thereof
- C08F4/659—Component covered by group C08F4/64 containing a transition metal-carbon bond
- C08F4/65908—Component covered by group C08F4/64 containing a transition metal-carbon bond in combination with an ionising compound other than alumoxane, e.g. (C6F5)4B-X+
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F4/00—Polymerisation catalysts
- C08F4/42—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors
- C08F4/44—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides
- C08F4/60—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
- C08F4/62—Refractory metals or compounds thereof
- C08F4/64—Titanium, zirconium, hafnium or compounds thereof
- C08F4/659—Component covered by group C08F4/64 containing a transition metal-carbon bond
- C08F4/65912—Component covered by group C08F4/64 containing a transition metal-carbon bond in combination with an organoaluminium compound
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F4/00—Polymerisation catalysts
- C08F4/42—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors
- C08F4/44—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides
- C08F4/60—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
- C08F4/62—Refractory metals or compounds thereof
- C08F4/64—Titanium, zirconium, hafnium or compounds thereof
- C08F4/659—Component covered by group C08F4/64 containing a transition metal-carbon bond
- C08F4/6592—Component covered by group C08F4/64 containing a transition metal-carbon bond containing at least one cyclopentadienyl ring, condensed or not, e.g. an indenyl or a fluorenyl ring

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)

AU15485/97A 1996-01-30 1997-01-30 Heteroatom substituted metallocene compounds for olefin polymerization catalyst systems and methods for preparing them Ceased AU722731B2 (en)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
FI960437A FI104826B (fi)	1996-01-30	1996-01-30	Heteroatomilla substituoituja metalloseeniyhdisteitä olefiinipolymerointikatalyytti-systeemejä varten ja menetelmä niiden valmistamiseksi
FI960437		1996-01-30
PCT/FI1997/000049 WO1997028170A1 (en)	1996-01-30	1997-01-30	Heteroatom substituted metallocene compounds for olefin polymerization catalyst systems and methods for preparing them

Publications (2)

Publication Number	Publication Date
AU1548597A AU1548597A (en)	1997-08-22
AU722731B2 true AU722731B2 (en)	2000-08-10

Family

ID=8545178

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
AU15485/97A Ceased AU722731B2 (en)	1996-01-30	1997-01-30	Heteroatom substituted metallocene compounds for olefin polymerization catalyst systems and methods for preparing them

Country Status (20)

Country	Link
US (1)	US6277778B1 (cs)
EP (1)	EP0880534B1 (cs)
JP (1)	JP4051089B2 (cs)
KR (1)	KR19990082158A (cs)
CN (1)	CN1089342C (cs)
AR (1)	AR005612A1 (cs)
AT (1)	ATE256691T1 (cs)
AU (1)	AU722731B2 (cs)
BR (1)	BR9707236A (cs)
CZ (1)	CZ297674B6 (cs)
DE (1)	DE69726841T2 (cs)
ES (1)	ES2212070T3 (cs)
FI (1)	FI104826B (cs)
HU (1)	HUP9902106A3 (cs)
IL (1)	IL125542A (cs)
MY (1)	MY120110A (cs)
SK (1)	SK285145B6 (cs)
TW (1)	TW442509B (cs)
WO (1)	WO1997028170A1 (cs)
ZA (1)	ZA97766B (cs)

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Publication number	Publication date
JP2000505794A (ja)	2000-05-16
FI104826B (fi)	2000-04-14
CZ229498A3 (cs)	1998-12-16
ATE256691T1 (de)	2004-01-15
US6277778B1 (en)	2001-08-21
JP4051089B2 (ja)	2008-02-20
HUP9902106A2 (hu)	1999-11-29
EP0880534A1 (en)	1998-12-02
DE69726841T2 (de)	2004-11-04
IL125542A (en)	2003-03-12
KR19990082158A (ko)	1999-11-25
CN1214687A (zh)	1999-04-21
CN1089342C (zh)	2002-08-21
MY120110A (en)	2005-09-30
AR005612A1 (es)	1999-06-23
ES2212070T3 (es)	2004-07-16
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BR9707236A (pt)	1999-07-20
FI960437L (fi)	1997-07-31
SK285145B6 (sk)	2006-07-07
AU1548597A (en)	1997-08-22
SK100898A3 (en)	1999-03-12
CZ297674B6 (cs)	2007-02-28
IL125542A0 (en)	1999-03-12
FI960437A0 (fi)	1996-01-30
TW442509B (en)	2001-06-23
EP0880534B1 (en)	2003-12-17
HUP9902106A3 (en)	2000-04-28
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Publication	Publication Date	Title
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